Evidence map›Paper›PMID 25723336›Full record

ArticleJournal of proteome research2015

Paraoxonase-3 is depleted from the high-density lipoproteins of autoimmune disease patients with subclinical atherosclerosis.

Judit Marsillach, Jessica O Becker, Tomas Vaisar, Bevra H Hahn, John D Brunzell, Clement E Furlong, Ian H de Boer, Maureen A McMahon, Andrew N Hoofnagle, DCCT/EDIC Research Group

Open access · greenAbstract read
In one paragraph

Article in Journal of proteome research, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
4.3field-weighted citation impact, top 5% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

33 citing papers in PubMed, 59 citations in OpenAlex.

  1. Trial
  2. Review
  3. Review
  4. Article
  5. Article
  6. The Paraoxonase (International journal of molecular sciences · 2025
    Review
  7. Article
  8. Review
  9. Review
  10. Review
  11. Review
  12. Article
  13. Review
  14. Review
  15. Cardiovascular disease in systemic lupus erythematosus.Rheumatology and immunology research · 2021
    Review
  16. Review
  17. Review
  18. Article
  19. Review
  20. Paraoxonase Role in Human Neurodegenerative Diseases.Antioxidants (Basel, Switzerland) · 2020
    Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors at 2 institutions in 1 country.

Judit Marsillach
Jessica O Becker
Tomas Vaisar
Bevra H Hahn§Department of Medicine (Division of Rheumatology), University of California Los Angeles, 1000 Veteran Avenue 32-59, Los Angeles, California 90095, United States.
John D Brunzell
Clement E Furlong⊥Department of Genome Sciences, University of Washington, 3720 Fifteenth Avenue Northeast, Seattle, Washington 98195, United States.
Ian H de Boer¶Kidney Research Institute, University of Washington, 325 Ninth Avenue, Seattle, Washington 98104, United States.
Maureen A McMahon§Department of Medicine (Division of Rheumatology), University of California Los Angeles, 1000 Veteran Avenue 32-59, Los Angeles, California 90095, United States.
Andrew N Hoofnagle¶Kidney Research Institute, University of Washington, 325 Ninth Avenue, Seattle, Washington 98104, United States.
DCCT/EDIC Research Group
University of Washington · USUniversity of California, Los Angeles · US

Funding

WILDLIFE BIOMARKER APPLICATIONS TO REMEDIATION DECISION MAKINGP42ES004696 · NIEHS · UNIVERSITY OF WASHINGTON · PI GALLAGHER, EVAN P · 1987 to 2021
$51.2M
Vector and Transgenic Mouse CoreP30DK017047 · NIDDK · UNIVERSITY OF WASHINGTON · PI Sakeneh Zraika · 1986 to 2026
$41.4M
PILOT STUDY--CLINICAL NUTRITION RESEARCHP30DK035816 · NIDDK · UNIVERSITY OF WASHINGTON · PI Ellen A Schur · 1986 to 2026
$30.4M
STUDY OF CELLULAR &MOLECULAR ASPECTS OF PESTICIDE NEURODEVELOPMENTAL TOXICITYP01ES009601 · NIEHS · UNIVERSITY OF WASHINGTON · PI FAUSTMAN, ELAINE M · 1999 to 2013
$8.7M
STRUCTURE/FUNCTION OF THE HUMAN PON1 POLYMORPHISMR01ES009883 · NIEHS · UNIVERSITY OF WASHINGTON · PI FURLONG, CLEMENT EUGENE · 1999 to 2013
$5.3M
The PREDICTS risk score for increased atherosclerosis and disease activity in SLER01AR063754 · NIAMS · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI MCMAHON, MAUREEN A · 2014 to 2018
$2.8M
HDL and cardiovascular risk in chronic kidney diseaseR01HL111375 · NHLBI · UNIVERSITY OF WASHINGTON · PI HOOFNAGLE, ANDREW N · 2012 to 2015
$1.5M
Pro-Inflammatory HDL as a Novel Target for the Indentification of AtherosclerosisK23AR053864 · NIAMS · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI MCMAHON, MAUREEN A · 2007 to 2011
$625k
NHLBI NIH HHS R01 HL111375NHLBI NIH HHS R01HL111375NIAMS NIH HHS K23 AR053864NIAMS NIH HHS K23AR053864NIAMS NIH HHS R01 AR063754NIDDK NIH HHS P30 DK017047NIDDK NIH HHS P30DK017047NIDDK NIH HHS P30 DK035816NIDDK NIH HHS P30DK035816NIEHS NIH HHS P01ES009601NIEHS NIH HHS P42 ES004696NIEHS NIH HHS R01 ES009883NIEHS NIH HHS R01ES09883
6 · The paper itself

Abstract

Patients with autoimmune diseases have a significantly increased risk of developing cardiovascular disease. In disease, high-density lipoprotein (HDL) particles lose their anti-inflammatory and antioxidant properties and become dysfunctional. The purpose of this study was to test the hypothesis that alterations in the HDL proteomic profile are associated with subclinical atherosclerosis and HDL dysfunction in patients with autoimmune diseases such as systemic lupus erythematosus (SLE) and type 1 diabetes. Targeted proteomics was used to quantify the relative abundance of 18 proteins in HDL from SLE patients with and without atherosclerotic plaque detectable by carotid ultrasound. Changes in the proteomic profile were compared against the in vitro ability of HDL to protect against lipid oxidation. The same proteins were quantified in HDL from patients with type 1 diabetes with or without coronary artery calcification as determined by computed tomography. In each population, paraoxonase-3 (PON3), a potent antioxidant protein, was depleted from the HDL of patients with subclinical atherosclerosis. PON3 expression in HDL was positively correlated with HDL antioxidant function. These results suggest that PON3 may be an important protein in preventing atherosclerosis and highlight the importance of antioxidant proteins in the prevention of atherosclerosis in vivo.

Indexed as

AdultAntioxidantsAryldialkylphosphataseCarotid ArteriesCase-Control StudiesChromatography, LiquidCohort StudiesDiabetes Mellitus, Type 1FemaleGene ExpressionHumansLipoproteins, HDLLupus Erythematosus, SystemicMaleMiddle AgedPlaque, AtheroscleroticAntioxidantsAryldialkylphosphataseLipoproteins, HDLPON3 protein, humancarotid plaquecoronary artery calcificationdysfunctionalhigh-density lipoproteinsmass spectrometryparaoxonase-3pro-inflammatorysystemic lupus erythematosustype 1 diabetes

Identifiers

PMID25723336
PMCPMC4434596
OpenAlexW1996682849

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.